Alportův syndrom
| Title in English | Alports syndrom |
|---|---|
| Authors | |
| Year of publication | 2014 |
| Type | Conference abstract |
| MU Faculty or unit | |
| Citation | |
| Description | Alports syndrom is a herital disability of bazal membrans (1:5000 inhabitions). Is characterised by nefropatia, kochlear handicap and by eye changes. Responsible is a production of abnormal chain of alfa colagen IV. |
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